ID

16717

Beskrivning

Sponsor: OSI Pharmaceuticals Information provided by (Responsible Party): Astellas Pharma Inc (OSI Pharmaceuticals) A multicenter, randomized, double-blind, placebo-controlled, phase 3 study of single-agent Tarceva® (erlotinib) following complete tumor resection with or without adjuvant chemotherapy in patients with stage IB-IIIA non-small cell lung carcinoma who have EGFR-positive tumors. See https://clinicaltrials.gov/ct2/show/NCT00373425 Part of study: Concomitant Medications

Länk

https://clinicaltrials.gov/ct2/show/NCT00373425

Nyckelord

  1. 2016-08-02 2016-08-02 -
  2. 2016-08-03 2016-08-03 - Julian Varghese
Uppladdad den

2 augusti 2016

DOI

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Licens

Creative Commons BY-NC 3.0 Legacy

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Concomitant Medications, Tarceva in NSCLC patients who have EGFR-positive tumors NCT00373425

Concomitant Medications, Tarceva in NSCLC patients who have EGFR-positive tumors NCT00373425

Concomitant Medications
Beskrivning

Concomitant Medications

Concomitant Medication
Beskrivning

Concomitant Medication

Datatyp

boolean

Alias
UMLS CUI [1]
C2347852
Vorherige Medikationen
Beskrivning

Vorherige Medikationen

Nummer des Medikaments
Beskrivning

Concomitant Medication

Datatyp

text

Alias
UMLS CUI [1]
C2347852
Prophylaxis
Beskrivning

Indication Prophylaxis

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2826696
UMLS CUI [1,2]
C0199176
Nummer des Medikaments
Beskrivning

Indication

Datatyp

text

Alias
UMLS CUI [1]
C2826696
Benützt der Patient dieses Medikament noch immer
Beskrivning

Concomitant Medication Start Date

Datatyp

boolean

Alias
UMLS CUI [1]
C2826734
Anfangsdatum
Beskrivning

Concomitant Medication Start Date

Datatyp

date

Alias
UMLS CUI [1]
C2826734
Benützt der Patient dieses Medikament noch immer
Beskrivning

Concomitant Medication End Date

Datatyp

boolean

Alias
UMLS CUI [1]
C2826744
Datum des Endes
Beskrivning

Concomitant Medication End Date

Datatyp

date

Alias
UMLS CUI [1]
C2826744

Similar models

Concomitant Medications, Tarceva in NSCLC patients who have EGFR-positive tumors NCT00373425

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Concomitant Medication
Item
boolean
C2347852 (UMLS CUI [1])
Item Group
Vorherige Medikationen
Concomitant Medication
Item
Nummer des Medikaments
text
C2347852 (UMLS CUI [1])
Indication Prophylaxis
Item
Prophylaxis
boolean
C2826696 (UMLS CUI [1,1])
C0199176 (UMLS CUI [1,2])
Indication
Item
Nummer des Medikaments
text
C2826696 (UMLS CUI [1])
Concomitant Medication Start Date
Item
Benützt der Patient dieses Medikament noch immer
boolean
C2826734 (UMLS CUI [1])
Concomitant Medication Start Date
Item
Anfangsdatum
date
C2826734 (UMLS CUI [1])
Concomitant Medication End Date
Item
Benützt der Patient dieses Medikament noch immer
boolean
C2826744 (UMLS CUI [1])
Concomitant Medication End Date
Item
Datum des Endes
date
C2826744 (UMLS CUI [1])

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